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1.
Epidemiol Infect ; 147: e20, 2018 10 08.
Article in English | MEDLINE | ID: mdl-30293540

ABSTRACT

A cluster of Salmonella Paratyphi B variant L(+) tartrate(+) infections with indistinguishable pulsed-field gel electrophoresis patterns was detected in October 2015. Interviews initially identified nut butters, kale, kombucha, chia seeds and nutrition bars as common exposures. Epidemiologic, environmental and traceback investigations were conducted. Thirteen ill people infected with the outbreak strain were identified in 10 states with illness onset during 18 July-22 November 2015. Eight of 10 (80%) ill people reported eating Brand A raw sprouted nut butters. Brand A conducted a voluntary recall. Raw sprouted nut butters are a novel outbreak vehicle, though contaminated raw nuts, nut butters and sprouted seeds have all caused outbreaks previously. Firms producing raw sprouted products, including nut butters, should consider a kill step to reduce the risk of contamination. People at greater risk for foodborne illness may wish to consider avoiding raw products containing raw sprouted ingredients.


Subject(s)
Disease Outbreaks , Salmonella Food Poisoning/epidemiology , Salmonella paratyphi B/pathogenicity , Seedlings/adverse effects , Vegetable Products/adverse effects , Adolescent , Adult , Age Distribution , Databases, Factual , Female , Food Safety , Humans , Incidence , Male , Middle Aged , Retrospective Studies , Risk Assessment , Salmonella Food Poisoning/etiology , Salmonella Food Poisoning/physiopathology , Sex Distribution , United States/epidemiology
2.
Forensic Sci Rev ; 24(2): 143-50, 2012 Jul.
Article in English | MEDLINE | ID: mdl-26244269

ABSTRACT

For the past two decades, forensic DNA analysis has rapidly expanded in both utility and value to criminal investigations. As the number of crime scene and convict/arrestee samples has continued to grow, many forensic DNA laboratories find themselves struggling to test samples in a timely fashion. Agencies employ various methods for calculating their sample intake and processing capacity, yet database and casework sample backlogs continue to present a major challenge. One issue many forensic laboratories face is limited availability of resources for training new analysts. High-quality training enables analysts to effectively perform various aspects of DNA profiling, and as such, it is essential to ensuring consistent, high-quality results. This is well documented in the guidelines established in the FBI's Quality Assurance Standards for Forensic DNA Testing Laboratories in the United States as well as internationally by agencies like INTERPOL. A facility dedicated to training analysts on both theoretical and practical aspects of automated sample processing accelerates the establishment and expansion of high-throughput forensic DNA laboratories. The present article will discuss various aspects of training and agencies that provide such training programs.

3.
Anim Genet ; 35(3): 213-9, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15147393

ABSTRACT

Sequence-based gene expression data are used to interpret results from functional genomic and proteomics studies. Although more than 300 000 bovine-expressed sequence tags (ESTs) are available in public databases, a more thorough and directed sampling of the expressed genome is needed to identify new transcripts and improve assembly and annotation of existing transcript sequences. Accordingly, we examined the utility of constructing cDNA libraries synthesized by arbitrarily primed RT-PCR of mRNA from tissues not well represented in the publicly available bovine EST database. A total of 33 cDNA libraries were constructed from healthy and infected mammary gland tissues of Brazilian Gir and Holstein cattle. This series of libraries was used to generate 6481 open reading frame-expressed sequence tags (ORESTES) that assembled into 1798 unique sequence elements of which, 1157 did not significantly match sequence assemblies available in the Bos taurus gene index. However, a total of 264 of these 1157 sequence elements aligned with mouse and human expressed sequences demonstrating that ORESTES is an effective resource for discovery of novel expressed sequences in cattle. Furthermore, comparison of the alignment position of bovine ORESTES-derived sequence elements to human gene reference sequences suggested that the priming events for cDNA synthesis more often occurred at the central portion of a transcript, which may have contributed to the relatively high rate of novel sequence discovery.


Subject(s)
Cattle/genetics , Expressed Sequence Tags , Gene Library , Mammary Glands, Animal/chemistry , Open Reading Frames/genetics , RNA, Messenger/genetics , Animals , Base Sequence , DNA Primers , Gene Expression , Humans , Molecular Sequence Data , Reverse Transcriptase Polymerase Chain Reaction , Sequence Analysis, DNA
4.
J Immunol Methods ; 84(1-2): 365-73, 1985 Nov 28.
Article in English | MEDLINE | ID: mdl-3905972

ABSTRACT

Knowledge that Treponema pallidum adhesin proteins bind to host fibronectin (Fn) via ligand-receptor interactions has resulted in development of an ELISA for measuring specific antitreponemal antibodies in sera of syphilitic patients and infected experimental animals. As little as 50 ng of T. pallidum total protein extract added to Fn-coated wells permitted half-maximal levels of ELISA reactivity. Detection of serum antibody from intratesticularly infected rabbits occurred at dilutions greater than 1/100,000. Antibody titers in serum from patients with primary and latent syphilis were positive at 1/1 000 dilutions while serum samples from patients with secondary syphilis were reactive at 1/10,000. Furthermore, the ELISA proved useful for evaluating serum samples from individuals with other treponemal infections. Antibodies raised against the non-pathogenic spirochete, T. phagedenis biotype Reiter, were non-reactive with Fn-T. pallidum complexes. Also, Reiter treponemal proteins did not bind to Fn-coated wells. This ELISA using Fn as a capture vehicle for treponemal adhesin proteins was superior to 3 other routinely used tests for syphilis diagnosis.


Subject(s)
Adhesins, Bacterial , Antibodies, Bacterial/analysis , Bacterial Proteins/immunology , Enzyme-Linked Immunosorbent Assay/methods , Syphilis Serodiagnosis/methods , Treponema pallidum/analysis , Animals , Antibody Specificity , Bacterial Proteins/isolation & purification , Bacterial Proteins/metabolism , Fibronectins/metabolism , Humans , Syphilis/immunology , Treponema pallidum/immunology , Yaws/immunology
5.
Chronobiologia ; 12(4): 361-5, 1985.
Article in English | MEDLINE | ID: mdl-3007053

ABSTRACT

The face fly, Musca autumnalis, exposed to shifts of an LD16:8 lighting schedule at varying intervals, whether previously untreated or given placebo or ACTH 1-17 treatment, before the initiation of shifts, exhibits an infradian frequency response in mortality. At overall 50% mortality, a periodicity of approximately 4.5 days is found for flies exposed to placebo or ACTH 1-17 as a response to the shift interval. As compared to controls, the mortality of flies treated with placebo or ACTH 1-17 is delayed. Not all shift schedules are detrimental; some are actually beneficial.


Subject(s)
Adrenocorticotropic Hormone/pharmacology , Diptera/drug effects , Light , Longevity/drug effects , Peptide Fragments/pharmacology , Periodicity , Animals , Circadian Rhythm/drug effects
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